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Medical Devices › Regulatory Requirements › Environmental Protection Agency (EPA)

Akin Gump Strauss Hauer & Feld LLP

Regulatory Relief for Certain Stationary Sources to Promote American Security with Respect to Sterile Medical Equipment (Trump EO...

Akin Gump Strauss Hauer & Feld LLP on

This proclamation addresses the EPA’s April 5, 2024 final rule, National Emission Standards for Hazardous Air Pollutants: Ethylene Oxide Emissions Standards for Sterilization Facilities Residual Risk and Technology Review, 89...more

Benesch

Dental/DSO Intelligence Monthly Report: March/April 2025

Benesch on

ADA Advocating for Fluoridation, Says Medical Devices Should Not Be Subjected to Tariffs - The dental industry and DSOs are experiencing change as both continue to embrace technology, including AI. The political and...more

Hogan Lovells

PRODUCT | PFAS and product law: Navigating regulatory and legal risks

Hogan Lovells on

Regulation and litigation surrounding per- and polyfluoroalkyl substances (PFAS) – a class of organic chemicals used in a variety of industrial and consumer products – is on the rise and evolving day-by-day. And the PFAS...more

DLA Piper

EPA Expands Mandatory Federal Purchasing Program

DLA Piper on

The US Environmental Protection Agency (EPA) recently announced that it is expanding its Recommendations of Specifications, Standards, and Ecolabels for Federal Purchasing Program (Recommendations Program) to include new...more

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